Fibrinogen Adsorption in the Diabetic Foot Syndrome and Peripheral Arterial Occlusive Disease: First Clinical Experience

: The elimination of fibrinogen from plasma improves plasma viscosity and whole‐blood viscosity. For extracorporeal adsorption of fibrinogen, the pentapeptide gly‐pro‐arg‐pro‐lys was coupled to sepharose CL‐4B. Adsorbers containing 135 ml of coupled sepharose CL‐4B were used to eliminate fibrinogen...

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Veröffentlicht in:Therapeutic apheresis 2001-10, Vol.5 (5), p.335-339
Hauptverfasser: Richter, Werner O., Jahn, Peter, Jung, Norbert, Nielebock, Erika, Tachezy, Hauke
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container_end_page 339
container_issue 5
container_start_page 335
container_title Therapeutic apheresis
container_volume 5
creator Richter, Werner O.
Jahn, Peter
Jung, Norbert
Nielebock, Erika
Tachezy, Hauke
description : The elimination of fibrinogen from plasma improves plasma viscosity and whole‐blood viscosity. For extracorporeal adsorption of fibrinogen, the pentapeptide gly‐pro‐arg‐pro‐lys was coupled to sepharose CL‐4B. Adsorbers containing 135 ml of coupled sepharose CL‐4B were used to eliminate fibrinogen from the plasma of 7 men and 3 women (48–75 years old). Nine patients suffered from diabetes mellitus, 1 patient from peripheral arterial occlusive disease, and 5 patients were on regular hemodialysis. Treatments were scheduled on Days 1, 2, 4, 6, 8, 10, 13, 16, 19, 22, 25, and 28. One hundred forty‐four treatments with fibrinogen adsorption were performed. No clinical side effects due to the fibrinogen adsorption procedure were observed. In these 10 patients, fibrinogen concentration before the first treatment was 473.7 ± 183.7 mg/dl. In the first treatment session, fibrinogen concentration was lowered to 241.4 ± 125.8 mg/dl by treating 4,270 ± 1,180 ml of plasma. In the following 134 treatments, the pretreatment concentration of fibrinogen was 262.6 ± 83.4 mg/dl, and the posttreatment concentration was 120.6 ± 37.2 mg/dl. The mean amount of plasma treated was 3,737 ± 1,643 ml, and the mean duration of a treatment session (except first treatment) was 143.7 ± 63.1 min. In 7 patients, a mean posttreatment fibrinogen concentration of ≤123 mg/dl was obtained; in the other patients, concentrations of 133, 177, and 184 mg/dl were obtained. Yet, the decrease of fibrinogen concentration was also pronounced in these 3 patients: −82%, −67%, and −73%, respectively. During the treatment period of 28 days, wound healing was observed in 9 of the 10 patients. In conclusion, affinity chromatography using the pentapeptide gly‐pro‐arg‐pro‐lys is an effective, selective, and safe procedure to lower fibrinogen concentration in plasma. It could be a therapeutic option in severe blood vessel disease in which drug therapy is not sufficient and invasive procedures such as bypass or angioplasty cannot be applied. Yet, more information is needed, for example, about the fibrinogen concentration that has to be reached to get the maximal improvement of micro‐ and/or macrocirculation.
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For extracorporeal adsorption of fibrinogen, the pentapeptide gly‐pro‐arg‐pro‐lys was coupled to sepharose CL‐4B. Adsorbers containing 135 ml of coupled sepharose CL‐4B were used to eliminate fibrinogen from the plasma of 7 men and 3 women (48–75 years old). Nine patients suffered from diabetes mellitus, 1 patient from peripheral arterial occlusive disease, and 5 patients were on regular hemodialysis. Treatments were scheduled on Days 1, 2, 4, 6, 8, 10, 13, 16, 19, 22, 25, and 28. One hundred forty‐four treatments with fibrinogen adsorption were performed. No clinical side effects due to the fibrinogen adsorption procedure were observed. In these 10 patients, fibrinogen concentration before the first treatment was 473.7 ± 183.7 mg/dl. In the first treatment session, fibrinogen concentration was lowered to 241.4 ± 125.8 mg/dl by treating 4,270 ± 1,180 ml of plasma. In the following 134 treatments, the pretreatment concentration of fibrinogen was 262.6 ± 83.4 mg/dl, and the posttreatment concentration was 120.6 ± 37.2 mg/dl. The mean amount of plasma treated was 3,737 ± 1,643 ml, and the mean duration of a treatment session (except first treatment) was 143.7 ± 63.1 min. In 7 patients, a mean posttreatment fibrinogen concentration of ≤123 mg/dl was obtained; in the other patients, concentrations of 133, 177, and 184 mg/dl were obtained. Yet, the decrease of fibrinogen concentration was also pronounced in these 3 patients: −82%, −67%, and −73%, respectively. During the treatment period of 28 days, wound healing was observed in 9 of the 10 patients. In conclusion, affinity chromatography using the pentapeptide gly‐pro‐arg‐pro‐lys is an effective, selective, and safe procedure to lower fibrinogen concentration in plasma. It could be a therapeutic option in severe blood vessel disease in which drug therapy is not sufficient and invasive procedures such as bypass or angioplasty cannot be applied. 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For extracorporeal adsorption of fibrinogen, the pentapeptide gly‐pro‐arg‐pro‐lys was coupled to sepharose CL‐4B. Adsorbers containing 135 ml of coupled sepharose CL‐4B were used to eliminate fibrinogen from the plasma of 7 men and 3 women (48–75 years old). Nine patients suffered from diabetes mellitus, 1 patient from peripheral arterial occlusive disease, and 5 patients were on regular hemodialysis. Treatments were scheduled on Days 1, 2, 4, 6, 8, 10, 13, 16, 19, 22, 25, and 28. One hundred forty‐four treatments with fibrinogen adsorption were performed. No clinical side effects due to the fibrinogen adsorption procedure were observed. In these 10 patients, fibrinogen concentration before the first treatment was 473.7 ± 183.7 mg/dl. In the first treatment session, fibrinogen concentration was lowered to 241.4 ± 125.8 mg/dl by treating 4,270 ± 1,180 ml of plasma. In the following 134 treatments, the pretreatment concentration of fibrinogen was 262.6 ± 83.4 mg/dl, and the posttreatment concentration was 120.6 ± 37.2 mg/dl. The mean amount of plasma treated was 3,737 ± 1,643 ml, and the mean duration of a treatment session (except first treatment) was 143.7 ± 63.1 min. In 7 patients, a mean posttreatment fibrinogen concentration of ≤123 mg/dl was obtained; in the other patients, concentrations of 133, 177, and 184 mg/dl were obtained. Yet, the decrease of fibrinogen concentration was also pronounced in these 3 patients: −82%, −67%, and −73%, respectively. During the treatment period of 28 days, wound healing was observed in 9 of the 10 patients. In conclusion, affinity chromatography using the pentapeptide gly‐pro‐arg‐pro‐lys is an effective, selective, and safe procedure to lower fibrinogen concentration in plasma. It could be a therapeutic option in severe blood vessel disease in which drug therapy is not sufficient and invasive procedures such as bypass or angioplasty cannot be applied. 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For extracorporeal adsorption of fibrinogen, the pentapeptide gly‐pro‐arg‐pro‐lys was coupled to sepharose CL‐4B. Adsorbers containing 135 ml of coupled sepharose CL‐4B were used to eliminate fibrinogen from the plasma of 7 men and 3 women (48–75 years old). Nine patients suffered from diabetes mellitus, 1 patient from peripheral arterial occlusive disease, and 5 patients were on regular hemodialysis. Treatments were scheduled on Days 1, 2, 4, 6, 8, 10, 13, 16, 19, 22, 25, and 28. One hundred forty‐four treatments with fibrinogen adsorption were performed. No clinical side effects due to the fibrinogen adsorption procedure were observed. In these 10 patients, fibrinogen concentration before the first treatment was 473.7 ± 183.7 mg/dl. In the first treatment session, fibrinogen concentration was lowered to 241.4 ± 125.8 mg/dl by treating 4,270 ± 1,180 ml of plasma. In the following 134 treatments, the pretreatment concentration of fibrinogen was 262.6 ± 83.4 mg/dl, and the posttreatment concentration was 120.6 ± 37.2 mg/dl. The mean amount of plasma treated was 3,737 ± 1,643 ml, and the mean duration of a treatment session (except first treatment) was 143.7 ± 63.1 min. In 7 patients, a mean posttreatment fibrinogen concentration of ≤123 mg/dl was obtained; in the other patients, concentrations of 133, 177, and 184 mg/dl were obtained. Yet, the decrease of fibrinogen concentration was also pronounced in these 3 patients: −82%, −67%, and −73%, respectively. During the treatment period of 28 days, wound healing was observed in 9 of the 10 patients. In conclusion, affinity chromatography using the pentapeptide gly‐pro‐arg‐pro‐lys is an effective, selective, and safe procedure to lower fibrinogen concentration in plasma. It could be a therapeutic option in severe blood vessel disease in which drug therapy is not sufficient and invasive procedures such as bypass or angioplasty cannot be applied. Yet, more information is needed, for example, about the fibrinogen concentration that has to be reached to get the maximal improvement of micro‐ and/or macrocirculation.</abstract><cop>Boston, MA, USA</cop><pub>Blackwell Science Inc</pub><pmid>11778917</pmid><doi>10.1046/j.1526-0968.2001.00335.x</doi><tpages>5</tpages></addata></record>
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subjects Adsorption
Aged
Arterial Occlusive Diseases - blood
Arterial Occlusive Diseases - therapy
Blood Component Removal - methods
Diabetic Foot - blood
Diabetic Foot - therapy
Diabetic foot syndrome
Female
Fibrinogen - therapeutic use
Fibrinogen adsorption
Humans
Male
Middle Aged
Peripheral arterial occlusive disease
Treatment Outcome
title Fibrinogen Adsorption in the Diabetic Foot Syndrome and Peripheral Arterial Occlusive Disease: First Clinical Experience
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